Пікірлер

• 
  @sameemas17232 сағат бұрын

  Bio-Rad assisted in the creation and release of COVID-19 . . .

• 
  @sameemas17232 сағат бұрын

  Bio-Rad created COVID-19 ?

• 
  @mannyadisa10 күн бұрын

  who designed that silly little comb that messes up my wells everytime i remove it 😹

• 
  @thamizh285018 күн бұрын

  How to read data table? What value needs to be considered for plotting graph?

• 
  @nancymullis335325 күн бұрын

  Kary and Bio-Rad had a great relationship, and he loved this song in its honor, and his of course. Love hearing it again! Thanks to Bio-Rad for all - Nancy Mullis

• 
  @ConCerN.exe.28 күн бұрын

  👍 Helpful

• 
  @Nicole72591Ай бұрын

  still loving the coloring book!

• 
  @uykusuzbirdoktor7879Ай бұрын

  herkes barış hocadan gelmiş sdkfnekjgh

• 
  @samiabdullah8044Ай бұрын

  سەرکەوتبێت مامۆستا هێدی😂❤

• 
  @a.s9509Ай бұрын

  Do you discard 100 microliters from the last (7th) microtube?

• 
  @umarabdulrazak4585Ай бұрын

  Thank you so much.

• 
  @botchjones1130Ай бұрын

  You have exposed arms while trying to be sterile? Cmon

• 
  @yama_no_ouАй бұрын

  can these pre-cast gels be used for observing nucleic acids?

• 
  @LasmiranАй бұрын

  mamosta hediw zaman 39 rozh pesh wizari........

• 
  @nvm7430Ай бұрын

  who's this Baris guy xd?

• 
  @krufxberk480Ай бұрын

  best anatomist in world

• 
  @nredirul5069Ай бұрын

  Bütün barış hoca yorumlarını beğendim👍

• 
  @aycelllaaaАй бұрын

  Barış hocam yollarsahoop buradayız

• 
  @TaraMishra-gs5ydАй бұрын

  Thank you for this video

• 
  @tnemakyildizАй бұрын

  hop barıs hocam

• 
  @BakariAzizАй бұрын

  Question: what is the purpose of the six "control samples" in the second well if we're using the first well as our standard/control?

• 
  @AlessioCapone2 ай бұрын

  Hi! Did I get it right that Stain-free blotting (in order to not make Ponceau) can be performed ONLY on Gels and not on membranes on the "ChemiDoc Touch System", while I can blot gels and membranes on "ChemiDoc MP"?

• 
  @claudeflex2 ай бұрын

  BARIŞ HOCAM ❤✋

• 
  @sevvalesi282 ай бұрын

  barış hocadan geldikk

• 
  @user-gp4ei5cs8m2 ай бұрын

  So helpful!! Thank you

• 
  @jyotiguleria12662 ай бұрын

  can i load one sigle set of plates contating gel and no dummy plate on the other side. Will it cause any problem in gel run

• 
  @JudyLehmbergEpicNature2 ай бұрын

  Absolutely the best song ever!!! You guys are seriously amazing! Thank you from a retired bio teacher!

• 
  @LeylaKonyal2 ай бұрын

  I'm coming from Barış hoca youtube chanel❤

• 
  @eylulvehayatindakiguzellikler2 ай бұрын

  barış hocamdan geldikkk

• 
  @busra92573 ай бұрын

  Came from "DR. BİYOLOJİ" chanel 🤙

• 
  @edwinabichedid96163 ай бұрын

  mos

• 
  @QaziAdeel3 ай бұрын

  Mr k

• 
  @_GandalfTheGrey_3 ай бұрын

  Wuhan needs to watch this video 😂

• 
  @afiyetolsun003 ай бұрын

  Barıs hoca kalitesiyle buradayız

• 
  @KishvarKhanam-qr1vl3 ай бұрын

  Durdarsan ki yaad aa gyi

• 
  @TrevonCoppin-ci1ig3 ай бұрын

  great vid !!!!!!!!

• 
  @khushiSingh-wu8tw3 ай бұрын

  Og song🥰🫶

• 
  @JYOtiRaNJanMANgaRaj3 ай бұрын

  ❤❤❤❤❤❤

• 
  @TJMsLe3 ай бұрын

  this is still my favorite of y'alls!

• 
  @anniem.k.94313 ай бұрын

  how does a dead cell that underwent apoptosis appear under the microscope? How to differentiate them from the healthy cells?

• 
  @tag72993 ай бұрын

  You can make a science of everything. Truth is, if you ain't looking for peak performance but just "get that plasmid into that damn cell", it'll be much easier. No need to make your productive lab life harder than it already is with overly correct academic BS, things that are done because they always have been done that way. and might yield 90% efficiency instead of 40%. The beauty of biology is, it can adapt and you as the experimenter usually don't fool around with DNA or cell amounts that leave it up to chance, there is plenty of biological redundancy at work to achieve your goal. Scrap the ice, you don't need it. You got your competent cells, just add your plasmid. Leave them sitting around thawed for a few minutes, then heatshock 30-60s at 42°C. Then put them into growth medium, ideally SOC, maybe LB, anything that nurtures them even if it might be some random soup broth. Let them have their way at ideal temperature for one or two replication cycles (Ecoli 30-40 minutes), then put them into the selective environment by streaking out or liquid inocculation. Longer incubation times will result in redundancy as transformed cells will proliferate, many colonies of the same type, makes it harder to plate select for the correct clone. Not a problem if you put them directly into liquid culture (of course no clone selectivity there, just faith). You could do that in your kitchen, when working with antibiotic resistances as usual. You don't even have to work in a sterile environment, just clean with sterile tools, ignore the laminar flow bench or the benchtop burner for your own convenience. If under these conditions you get contamination on your plates, you got bigger problems than that.

• 
  @aryanaliasif71214 ай бұрын

  Hello guys .

• 
  @asharahtsham50384 ай бұрын

  💀

• 
  @Jaberpro74 ай бұрын

  Yoo aryan ☠️

• 
  @yksascisi4 ай бұрын

  Barış hocam 🤟🤟

• 
  @walidnadirulahnaf39784 ай бұрын

  1. siapkan sub sel mini 2. sejajarkan gel sehingga sumur paling dekat dengan elektrode negatif 3. tempatkan egl agarosa ke ruang gel 4. tambahkan buffer elektroforesis ke reservoir sampai reservoir tertutup buffer elektroforesis sedalam 2mm 5. tempatkan sampel sesuai urutan yang benar 6. tempatkan sampel ke dalam sumur dengan menggunakan mikropipet. jagalah pipet tetep tegak lurus terhadap lubang 7. pasang tutup ruang gel sesuai dengan elektrodanya (hitam ke hitam, merah ke merah) 8. sambungkan elektrode ke catu daya 9. nyalakan catu daya 10. atur tegangan konstan sebesar 100V 11. atur timer menjadi 60s 12. amati perubahan yang terjadi

• 
  @monkeynuts51864 ай бұрын

  Who else in here for biotech

• 
  @vialoxn4 ай бұрын

  Thank you so much!

• 
  @roseofheaven_4 ай бұрын

  Dr Biyoloji🫡

• 
  @beanheadr4 ай бұрын

  Interesting that this process has not changed much over the years. I did a high school internship at the Kennedy Krieger Institute back in the late 90's working with X-ALD with mice as our catalyst. I remember being nervous using ethidium bromide after my lab director explained that exposure to it could cause my DNA to mutate!

• 
  @esra.7934 ай бұрын

  Barış Hocamda Barış Hocam

• 
  @loicgonzalez18904 ай бұрын

  What about psi differences ? Im stuck with this troubleshooting Please help

• 
  @leewilliam34174 ай бұрын

  Thankyou 😊